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    Release of trace elements during bioreductive dissolution of magnetite from metal mine tailings: potential impact on marine environments
    (Elsevier, 2021-09-20)
    Adverse impacts of mine tailings on water and sediments quality are major worldwide environmental problems. Due to the environmental issues associated with the deposition of mine tailings on land, a controversial discussed alternative is submarine tailings disposal (STD). However, Fe(III) bioreduction of iron oxides (e.g., magnetite) in the tailings disposed might cause toxic effects on coastal environments due to the release of different trace elements (TEs) contained in the oxides. To study the extent and kinetics of magnetite bioreduction under marine conditions and the potential release of TEs, a number of batch experiments with artificial seawater (pH 8.2) and a marine microbial strain ( Shewanella loihica ) were performed using several magnetite ore samples from different mines and a mine tailings sample. The elemental composition of the magnetite determined in the tailings showed relatively high amounts of TEs (e.g., Mn, Zn, Co) compared with those of the magnetite ore samples (LA-ICP-MS and EMPA analyses). The experiments were conducted at 10 °C in the dark for up to 113 days. Based on the consumption of lactate and production of acetate and aqueous Fe(II) over time, the magnitude of Fe(III) bioreduction was calculated using a geochemical model including Monod kinetics. Model simulations reproduced the release of iron and TEs observed throughout the experiments, e.g., Mn (up to 203 μg L −1 ), V (up to 79 μg L −1 ), As (up to 17 μg L −1 ) and Cu (up to 328 μg L −1 ), suggesting a potential contamination of pore water by STD. Therefore, the results of this study can help to better evaluate the potential impacts of STD.
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    Structural, hyperfine, and magnetic evolution of a natural magnetite–serpentine composite: Effects of magnetic separation and thermal treatment
    (Elsevier BV, 2026-08-15)
    In this work, the structural, hyperfine, and magnetic evolution of a natural magnetite–serpentine composite was systematically investigated in its as-collected state, after magnetic separation, and following thermal treatments. X-ray diffraction combined with Rietveld refinement reveals a lizardite-dominated matrix containing magnetite as the primary magnetic phase. Mössbauer spectroscopy identifies Fe2+ and Fe3+ cations distributed over distinct octahedral and tetrahedral sites in both lizardite and magnetite, providing insight into cation distribution and oxidation state evolution. Magnetic measurements reveal ferrimagnetic behavior dominated by magnetite, with a saturation magnetization of ∼79 emu g−1 at room temperature. The transition temperature was estimated from the derivative of the ZFC–FC magnetization curve with respect to temperature, which exhibits a relatively broad peak associated with the Verwey transition (118 K). This feature suggests the presence of relatively preserved magnetite within the ultramafic matrix, although the broad character of the transition may reflect structural disorder, particle-size effects, or magnetic interactions. In addition, the magnetic data indicate the coexistence of superparamagnetic behavior and possible spin-glass-like contributions, likely associated with surface disorder and nanoscale magnetic interactions. Water-assisted magnetic separation enhances the magnetic fraction, confirming that magnetite particles are embedded within the lizardite matrix. Thermal treatments at 500 °C and 1000 °C induce progressive dehydroxylation, oxidation of iron-bearing phases, and the formation of hematite, forsterite, silica, and clinoenstatite, leading to significant modifications in both hyperfine parameters and magnetic behavior. The results establish clear structure-hyperfine-magnetic correlations and demonstrate how magnetic separation and thermal processing govern the phase stability and functional magnetic response of natural magnetite–serpentine systems.
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    Comparative study of iron and trace element mobilization during Fe-oxide bioreduction in mine tailings: a case study of Ensenada Chapaco (Chile) and Portman Bay (Spain): Bioreduction and metal release in mine-tailings
    (Universitat de Barcelona, 2025-01-01)
    elements (e.g. Ti, Ni, Cd, Pb), leading to contamination of the marine environment. Sea-Tailings Disposal (STD) along the northern coast of Chile (Ensenada Chapaco) and along the eastern coast of Spain (Portman Bay) results in an adverse impact on the environment. This paper focuses on bioreduction under marine conditions. To this end, two column experiments were carried out with samples from Portman Bay and Ensenada Chapaco. Lactate (i.e. organic matter source) was supplied during the experiments. The results obtained are compared with those from batch experiments performed under similar conditions.In the column filled with Portman Bay tailings, the high content of magnetite (15wt%) in contact with water gives rise to a large magnetite surface area and abundant Fe(III), which results in a high release of Fe(II) and Trace Elements (TE). Since Fe(II) adsorbs onto the magnetite surface reducing the availability of Fe(III), the magnetite bioreduction and the consequent TE release decrease after 2000h. By contrast, the magnetite bioreduction lasts longer (3000h) in the column with Ensenada Chapaco tailings. This is because a lower magnetite content in the tailings (1wt%) provides a smaller reactive surface area yielding less Fe(III). Consequently, the concentrations of Fe(II) and TE in the output solutions are lower, which slows down the Fe(II) adsorption onto magnetite. This results in a longer magnetite bioreduction. Bioreduction is regulated by the availability of Fe(III) in both columns.It is inferred that the bioreduction rate diminishes as a function of time and increases as a function of soluble Fe(II) concentration. Moreover, the concentrations of TE released from the two bioreduced tailings exceed the elemental concentrations under marine conditions.
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    Comparative Study of Iron and Trace Element Mobilization during Fe-Oxide Bioreduction in Mine Tailings: a case study of Ensenada Chapaco (Chile) and Portman Bay (Spain)
    (Cartographic and Geological Institute of Catalonia, 2025-02-01)
    elements (e.g. Ti, Ni, Cd, Pb), leading to contamination of the marine environment. Sea-Tailings Disposal (STD) along the northern coast of Chile (Ensenada Chapaco) and along the eastern coast of Spain (Portman Bay) results in an adverse impact on the environment. This paper focuses on bioreduction under marine conditions. To this end, two column experiments were carried out with samples from Portman Bay and Ensenada Chapaco. Lactate (i.e. organic matter source) was supplied during the experiments. The results obtained are compared with those from batch experiments performed under similar conditions.In the column filled with Portman Bay tailings, the high content of magnetite (15wt%) in contact with water gives rise to a large magnetite surface area and abundant Fe(III), which results in a high release of Fe(II) and Trace Elements (TE). Since Fe(II) adsorbs onto the magnetite surface reducing the availability of Fe(III), the magnetite bioreduction and the consequent TE release decrease after 2000h. By contrast, the magnetite bioreduction lasts longer (3000h) in the column with Ensenada Chapaco tailings. This is because a lower magnetite content in the tailings (1wt%) provides a smaller reactive surface area yielding less Fe(III). Consequently, the concentrations of Fe(II) and TE in the output solutions are lower, which slows down the Fe(II) adsorption onto magnetite. This results in a longer magnetite bioreduction. Bioreduction is regulated by the availability of Fe(III) in both columns.It is inferred that the bioreduction rate diminishes as a function of time and increases as a function of soluble Fe(II) concentration. Moreover, the concentrations of TE released from the two bioreduced tailings exceed the elemental concentrations under marine conditions.
      1
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    Tailoring the Properties of Magnetite/PLA Nanocomposites: A Composition-Dependent Study
    (Multidisciplinary Digital Publishing Institute (MDPI), 2025)
    This study focused on composites of magnetite magnetic nanoparticles (MNP) and poly(lactic acid) (PLA) prepared via sonochemical synthesis. The evaluation of MNP loadings (2, 5, 10, 15, and 20 wt.%) provided insights into the structural and reactivity properties of the materials. Methods used included XRD, FT-IR and Raman spectroscopy, SEM and TEM microscopy, textural and thermal analysis (TG and DTA), and magnetic property measurements. The agreement between theoretical and experimental MNP loadings was good. XRD patterns showed predominantly MNP and semicrystalline phases, with a minor maghemite phase detected by FT-Raman and magnetic measurements. FT-IR analysis revealed interactions between MNP and PLA, confirmed by thermal analysis showing higher transition temperatures for the composites (145 °C) compared to pure PLA (139 °C). FT-Raman spectra also indicated that PLA helps prevent iron oxide oxidation, enhancing nanoparticle stability. SEM and TEM micrographs showed well-dispersed, spherical nanoparticles with minimal agglomeration, dependent on MNP loading. The nanocomposites exhibited low N₂ adsorption, resulting in low surface area (~2.1 m²/g) and porosity (~0.03 cm³/g). Magnetic analysis indicated that in the 2MNP/PLA sample, MNP were in a superparamagnetic-like regime at 300 K, suggesting good dispersion of 2 wt.% MNP in the PLA matrix.
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